摘要
以矮牵牛(Petunia hyvrida Vilm)叶片作为外植体。实验表明矮牵牛快速繁殖诱导分化培养基为Ms+6-BA1.0mg/L+NAA0.5mg/L。生根培养基为1/2MS+IBA0.1mg/L。试管苗移栽最合适的基质是珍珠岩。
The experiment was conducted using leaves as the explant. The experiment result shows that MS + 6 + BA1 . 0mg/L + NAA0 . 5 mg/L is suitable medium for the rapid propagation . Rooting medium is 1/2 MS + IBA 0.1 mg/L. Pertile is the best rooting medium.
出处
《新疆农业科学》
CAS
CSCD
2005年第B06期111-112,共2页
Xinjiang Agricultural Sciences
基金
乌鲁木齐县特色精品园艺高效示范(2003022A09)
